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"Le Pulse" Retis thrombus removal catheter - Taiwan Registration db842529e7939126a1d4957771dd1b23

Access comprehensive regulatory information for "Le Pulse" Retis thrombus removal catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number db842529e7939126a1d4957771dd1b23 and manufactured by LEMAITRE VASCULAR, INC.. The authorized representative in Taiwan is HSIN TUNG MEDICAL CO., LTD..

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db842529e7939126a1d4957771dd1b23
Registration Details
Taiwan FDA Registration: db842529e7939126a1d4957771dd1b23
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Device Details

"Le Pulse" Retis thrombus removal catheter
TW: โ€œๆจ‚่„ˆโ€้›ท็ทนๆ–ฏ่ก€ๆ “ๆธ…้™คๅฐŽ็ฎก
Risk Class 2

Registration Details

db842529e7939126a1d4957771dd1b23

DHA00602231303

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.5150 ่ก€ๆ “ๅˆ‡้™ค่ก“ๅฐŽ็ฎก

import

Dates and Status

May 16, 2011

May 16, 2026